Haiyan Kangyuan Medical Chida Co., Ltd. idapeza bwino satifiketi ya EU Medical Instruments (EU 2017/745, yotchedwa "MDR") pa February 1, 2023, nambala ya satifiketi ndi 6122159CE01, ndipo kuchuluka kwa ziphaso kumaphatikizapo Endotracheal Tubes for Single Use, Catheter Wosabala Kamodzi, Masks Oxygen Ogwiritsidwa Ntchito Pamodzi, Makanula a Oxygen a Nasal Ogwiritsidwa Ntchito Pamodzi, Guedel Airways Yogwiritsidwa Ntchito Pamodzi, Laryngeal Mask Airways, Masks a Anesthesia Ogwiritsidwa Ntchito Pamodzi, Zosefera Zopumira Zogwiritsa Ntchito Pamodzi, Mabwalo opumira Ogwiritsa Ntchito Pamodzi.

Akuti EU Medical Instrument Regulation MDR (EU 2017/745) idayamba kugwira ntchito pa Meyi 25, 2017, m'malo mwa Medical Instrument Directive MDD (93/42/EEC) ndi Active Implantable Medical Instrument Directive AIMDD (90/385). /EEC ), cholinga chake chokhazikitsa ndondomeko yoyendetsera bwino komanso yokhwima kuti iteteze bwino thanzi ndi chitetezo cha anthu ndi odwala. Pakati pawo, MDR yaika patsogolo zofunika kwambiri kwa opanga zida zachipatala pankhani ya kasamalidwe ka chiwopsezo cha zinthu, magwiridwe antchito ndi miyezo yachitetezo, kuwunika kwachipatala, komanso kuchenjeza ndi kuyang'anira pambuyo pa msika. Poyerekeza ndi malangizo a MDD, MDR yoyang'anira ili ndi kuyang'anira kolimba, kutsimikizira zovuta kwambiri, ndipo imayang'ana kwambiri chitetezo ndi mphamvu yazinthu.

Kangyuan Medical wakhala bwinobwino analandira MDR satifiketi nthawi ino, zimene zikutsimikizira kuti Kangyuan mankhwala afika kuzindikira EU ndi misika yapadziko lonse mwa mawu a ulamuliro kupanga, chitsimikizo khalidwe ndi kasamalidwe chiopsezo.

Kwa Kangyuan Medical, yomwe yakhala ikukhudzidwa kwambiri ndi msika waku Europe kwazaka zopitilira khumi, kupeza satifiketi ya MDR ndichinthu chofunikira kwambiri. , Latin America ndi misika ina inapereka chithandizo champhamvu.